A Non-interventional Study of Participants With BPDCN Treated With Chemotherapy

Condition(s) studied

Investigational drug(s) / intervention(s)

Chemotherapy: Several chemotherapy regimens can be considered (acute myeloid leukemia-like, acute lymphocytic leukemia-like, lymphoma-like). The choice of the regimen, as well as dosing and schedules, are based on the institution's and the health care provider's preferences. No study medication will be provided by the sponsor during this study.

Study summary

The main goal of this study is to investigate the effectiveness and safety of chemotherapy agents in the treatment of participants with BPDCN and to provide comparator arm data to the prospective ELZONRIS registry study (STML-401-0521).

Eligibility

Primary outcome measure(s)

• Objective Response Rate — Baseline through Month 18
• Composite Complete Response — Baseline through Month 18
• Number of Participants Bridged to Stem Cell Transplant — Baseline through Month 18
• Duration of Response — Baseline through Month 18
• Real-world Progression-free Survival — Baseline through Month 18
• Overall Survival — Baseline through Month 18
• Number of Participants with Treatment-emergent Adverse Events — Baseline through Month 18
• Number of Participants Requiring Transfusions — Baseline through Month 18
• Duration of Treatments Received and Hospitalization — Baseline through Month 18

Trial sites (67)

+ 27 more sites — see the full list on the official registry below.

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